A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14271799



Internal ID22197854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:16959885..16987300hg38UCSC Ensembl
Outerchr3:17001377..17028792hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222906
Supporting Variants
SamplesHG00732
Known GenesPLCL2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14271799
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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